Kreosotum
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Kreosotum
- Generic name
- WOOD CREOSOTE
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 8619e4e5-0c55-45db-e053-2a91aa0aa6b7
- SPL ID
- 0a0e390d-fe5e-9dc6-e063-6294a90a5f58
- Version
- 2
- Effective date
- 2023-11-13
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:43:31
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Kreosotum | openfda.brand_name | |
| generic name | WOOD CREOSOTE | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-2940-41 | openfda.package_ndc |
| ndc | product | 0220-2940 | openfda.product_ndc |
| ndc11 | package | 00220294041 | derived:openfda.package_ndc |
| spl id | 0a0e390d-fe5e-9dc6-e063-6294a90a5f58 | id | |
| spl set id | 8619e4e5-0c55-45db-e053-2a91aa0aa6b7 | set_id | |
| unii | 3JYG22FD73 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.